FDAFDA recall D-0769-2026 · Aug 19, 2026
Buy-Herbal: Kian Pee Wan Capsules recall
Recall found
Product
Kian Pee Wan Capsules, 30-count bottles
Reason for recall
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class I: FDA's most serious class, where use of or exposure to the product may cause serious health problems or death.
- Status
- Ongoing
- Codes, lots and dates
- All lots within expiry.
- Quantity
- 71 bottles
- Distribution
- Product was sold to individual consumers via ebay third party seller.
- Recalling firm
- Buy-Herbal, Flushing, NY
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-03-21
Source: openFDA enforcement record D-0769-2026 · search recall number D-0769-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.